| NDC包装代码 | 产品NDC | 产品类型 | 商品名 | 通用名 | 剂型 | 给药途径 | 上市日期 | 结束日期 | 市场类别 | 申请号 | 标签持有者 | 活性成分 | 规格 | 包装描述 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 68084-345-21 | 68084-345 | HUMAN PRESCRIPTION DRUG | Topiramate | Topiramate | TABLET, FILM COATED | ORAL | 20090413 | N/A | ANDA | ANDA078235 | American Health Packaging | TOPIRAMATE | 200 mg/1 | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-345-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-345-11) |
| 71335-1116-6 | 71335-1116 | HUMAN PRESCRIPTION DRUG | topiramate | topiramate | TABLET, FILM COATED | ORAL | 20220708 | N/A | ANDA | ANDA078235 | Bryant Ranch Prepack | TOPIRAMATE | 200 mg/1 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1116-6) |